Selection of Immunosuppression in Kidney Transplant Recipients Depending on Pre-transplant Donor-specific T-cell Reactivity.

Phase 4

Completed

• Conditions: Disorder Related to Renal Transplantation
• Interventions: Drug: PRE-TRANSPLANT (PRE=before)

• Registration Number: NCT01195194
• Lead Sponsor: Josep M Grinyo

Brief Summary

The objective is to assess if low pre-transplantation donor specific T-cell reactive patients measured by Enzyme-linked immunosorbent spot (ELISPOT)assay can be safely managed with Calcineurin inhibitor(CNI)-free Sirolimus(SRL)-based immunosuppression.

Detailed Description

Non randomized, pilot, prospective, open-label trial.

Study Timeline

• Study Start: 2008-03
• Study First Submitted: 2010-04-19
• Study First Submitted QC: 2010-09-03
• Study First Posted: 2010-09-06
• Primary Completion: 2012-06
• Study Completion: 2013-06
• Status Verified: 2014-02
• Last Update Submitted: 2014-02-24
• Last Update Posted: 2014-02-25

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 61

Inclusion Criteria

1. Age of donor and recipient between 18 and 65 years.
2. End-stage renal disease and scheduled to receive a primary or secondary renal allograft from a cadaveric, a living-unrelated, or a living-related donor. Patients scheduled for a second transplant must have maintained their primary graft for at least 6 months after transplantation, with the exception of graft failure due to technical reasons.
3. Panel reactive antibody (PRA) ≤ 20%, with negative standard cross-match.
4. Women of childbearing potential must have a negative serum pregnancy test before randomization.
5. Women of childbearing potential must agree to use a medically acceptable method of contraception throughout the treatment period and for 3 months following discontinuation of assigned treatment.
6. Signed and dated informed consent prior to transplantation.

Exclusion Criteria

1. Multiple organ transplants
2. Recipients of adult or pediatric en bloc kidney transplants or dual transplantation or non-heart beating donors.
3. Evidence of active systemic or localized major infection.
4. Evidence of infiltrate, cavitation, or consolidation on chest x-ray obtained during the screening/baseline evaluation.
5. Use of any investigational drug or treatment up to 4 weeks prior to transplantation.
6. Treatment with voriconazole, ketoconazole, itraconazole, fluconazole, clotrimazole, astemizole, pimozide, terfenadine, erythromycin, clarithromycin, telithromycin, troleandomycin, rifampin, rifabutin, or St. John's Wort that is not discontinued prior to randomization.
7. Treatment with aminoglycosides, amphotericin B, cisplatin, cisapride, metoclopramide, cimetidine, bromocriptine, danazol, or other drugs associated with renal dysfunction that are not discontinued prior to randomization.
8. Subjects with a screening/baseline total white blood cell count < 2,000/mm3 or absolute neutrophil count (ANC) < 500, platelet count < 100,000/mm3.
9. Fasting triglycerides > 400 mg/dL (> 4.6 mmol/L) or fasting total cholesterol > 300 mg/dL (> 7.8 mmol/L) despite optimal lipid-lowering therapy.
10. History of malignancy within 2 years of enrollment (except for adequately treated basal cell or squamous cell carcinoma of the skin).
11. Auto-immune diseases inactive immunosuppressive treatment ( 3 months prior to inclusion).
12. Patient with psychiatric disorders that could be non-compliance for the treatment.
13. Non Caucasian patients.
14. Active peptic ulcers that could produce intestinal absorption disorders.
15. Subjects who are known to be human immunodeficiency virus(HIV) or hepatitis B virus (HBV) positive. Patients with hepatitis C virus (HCV) positive should be excluded if polymerase chain reaction (PCR) positive or transaminates values are ≥2 upper normal value (UNV).
16. Diabetic patients.
17. Body mass index higher than 30 Kg/m2.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
A- negative pre-transplant ELISPOT	PRE-TRANSPLANT (PRE=before)	Sirolimus: Start at 5 mg/day as soon as treatment allocation arrives to obtain targeting levels to 8 -15 ng/ml (immunoassay) in the first 3 months, followed by trough levels of 5-10 ng/ml.
B- Positive pre-transplant ELISPOT	PRE-TRANSPLANT (PRE=before)	Tacrolimus 0.1 mg/kg/12h starting as soon as treatment allocation arrives to obtain targeting troughs levels of 8-15 ng/ml the first 3 months, followed by trough levels of 5-10 ng/ml until the end of the study.

Primary Outcome Measures

Name	Time	Method
Percentage of biopsy-confirmed acute rejection episodes	6 months	To describe cumulative biopsy-confirmed acute rejection in both groups by intention to treat analysis.

Secondary Outcome Measures

Name	Time	Method
Proteinuria measured in g/day	12 months	To describe proteinuria in g/day in both groups by intention to treat analysis.
Histology at month 6 protocol kidney allograft biopsy	6 months	To describe histology at month 6 in both groups by intention to treat and "on therapy" analysis.
Percentage of patients with negative ELISPOT	12 months	To describe percentage of patients with negative ELISPOT in both groups by intention to treat and "on therapy" analysis.
Percentage of patients in group A requiring CNI introduction.	24 months	To describe the percentage of patients in group A requiring CNI introduction.
Percentage of patients presenting adverse events requiring study withdrawal	24 months	To describe adverse events in the whole group ("screening failure" plus "intention to treat") in both treatments groups.
Percentage of biopsy-confirmed acute rejection episodes	12 months	To describe cumulative biopsy-confirmed acute rejection in both groups by intention to treat analysis.
Percentage of steroid-sensitive acute rejections rejection episodes	12 months	To describe the percentage of steroid-sensitive acute rejections rejection in both groups by intention to treat analysis.
Percentage of acute rejection episodes requiring treatment with antilymphocyte antibodies	12 months	To describe the need for antibody treatment in acute rejection episodes in both groups by intention to treat analysis.
Percentage of steroid-sensitive acute rejection episodes	6 months	To describe the percentage of steroid-sensitive acute rejections rejection in both groups by intention to treat analysis.
Percentage of acute rejection episodes requiring treatment with antilymphocyte antibodies.	6 months	To describe the need for antibody treatment in acute rejection episodes in both groups by intention to treat analysis.
Renal function estimated by Modification of Diet in Renal Disease (MDRD) formula.	12 months	To describe renal function measured by MDRD in both groups by intention to treat and "on therapy" analysis.

Trial Locations

Locations (2)

Nephrology Department. Hospital de Bellvitge; 🇪🇸 L'Hospitalet de Llobregat, Barcelone, Spain

Nephrology Department. Hospital Vall d'Hebró; 🇪🇸 Barcelona, Spain